Bathophenanthroline compound and process for preparing same

ABSTRACT

A novel bathophenanthroline compound of the general formula [I] or [II] is provided  
                 
 
wherein R 1  and R 2  may be the same or different and independently represent a linear, branched or cyclic, saturated or unsaturated hydrocarbon group, or a substituted or unsubstituted, saturated or unsaturated hydrocarbon group provided that at least one of R 1  and R 2  has at least two carbon atoms, and wherein Ar 1  and Ar 2  may be the same or different and independently represent a substituted or unsubstituted aryl group. A process for preparing the compound is also provided wherein bathophenanthroline and an organolithium compound are subjected to nucleophilic substitution reaction to obtain the compound of the above formula [I] or [II].

BACKGROUND OF THE INVENTION

This invention relates to a bathophenanthroline compound, which isadapted for use in an organic electroluminescent device (e.g. an organicelectroluminescent device suitable as a display device or alight-emitting device such as a spontaneous light flat display,especially an organic electroluminescent color display using an organicthin film as an electroluminescent layer), and also a process forpreparing the compound.

In recent years, importance of interfaces between human beings andmachines including multimedia-oriented commercial articles is exalted.For more comfortable and more efficient machine operations, it isnecessary to retrieve information from an operated machine withoutfailure simply, instantaneously and in an adequate amount. To this end,studies have been made on various types of display devices or displays.

As machines are now miniaturized, there is an increasing demand, day byday, for miniaturization and thinning of display devices. For instance,there is an inconceivable development with respect to theminiaturization of lap top-type information processors of the all-in-onetype such as notebook-size personal computers, notebook-size wordprocessors and the like. This, in turn, entails a remarkable technicalinnovation on liquid crystal displays for use as a display device forthe processor.

Nowadays, liquid crystal displays are employed as an interface of adiversity of articles and have wide utility in the fields not only oflap top-type information processors, but also of articles for our dailyuse including small-sized television sets, watches, desk-top calculatorsand the like.

These liquid crystal displays have been studied as a key of displaydevices, which are used as the interface connecting a human being and amachine and cover small-sized to large capacitance display devices whilemaking use of the feature that liquid crystals are low in drive voltageand power consumption. However, liquid crystal displays have theproblems that they do not rely on spontaneous light and thus need agreater power consumption for back light drive than for liquid crystaldrive, with the result that a service time is shortened when using abuilt-in battery, thus placing a limitation on their use. Moreover, theliquid crystal display has another problem that it has such a narrowangle of field as not to be suitable for use as a large-sized displaydevice.

Furthermore, the liquid crystal display depends on the manner of displayusing the orientation of liquid crystal molecules, and this isconsidered to bring about a serious problem that its contrast changesdepending on the angle even within an angle of field.

From the standpoint of drive systems, an active matrix system, which isone of drive systems, has a response speed sufficient to deal with amotion picture. However, since a TFT (thin film transistor) drivecircuit is used, a difficulty is involved in making a large screen sizeowing to the pixel defects, thus being disadvantageous in view of thereduction in cost.

In the liquid crystal display, a simple matrix system, which is anothertype of drive system, is not only low in cost, but also relatively easyin making a large screen size. However, this system has the problem thatits response speed is not enough to deal with a motion picture.

In contrast, a spontaneous light display device is now under study suchas on a plasma display device, an inorganic electroluminescent device,an organic electroluminescent device and the like.

The plasma display device employs plasma emission in a low pressure gasfor display and is suited for the purposes of a large size and largecapacitance, but has the problem on thinning and costs. In addition, anAC bias of high potential is required for its drive, and thus, thedisplay is not suitable as a portable device.

The inorganic electroluminescent device has been put on the market as agreen light emission display. Like the plasma display device, an AC biasdrive is essential, for which several hundreds of volts are necessary,thus not being of practical use.

In this connection, however, emission of three primaries including red(R), green (G) and blue (B) necessary for color display has beensucceeded due to the technical development. Since inorganic materialsare used for this purpose, it has been difficult to control emissionwavelengths depending on the molecular design or the like. Thus, it isbelieved that full color display is difficult.

On the other hand, the electroluminescent phenomenon caused by organiccompounds has been long studied ever since there was discovered aluminescent or emission phenomenon wherein carriers are injected intothe single crystal of anthracene capable of emitting a strongfluorescence in the first part of 1960s. However, such fluorescence islow in brightness and monochronous in nature, and the single crystal isused, so that this emission has been made as a fundamental investigationof carrier injection into organic materials.

However, since Tang et al. of Eastman Kodak have made public an organicthin film electroluminescent device of a built-up structure having anamorphous luminescent or emission layer capable of realizing low voltagedrive and high brightness emission in 1987, extensive studies have beenmade, in various fields, on the emission, stability, rise in brightness,built-up structure, manner of fabrication and the like with respect tothe three primaries of R, G and B.

Furthermore, diverse novel materials have been prepared with the aid ofthe molecular design inherent to an organic material. At present, itstarts to conduct extensive studies on applications, to color displays,of organic electroluminescent devices having excellent characteristicfeatures of DC low voltage drive, thinning, and spontaneous lightemission and the like.

The organic electroluminescent d vice (which may be sometimes referredto as organic EL device hereinafter) has a film thickness of 1 μm orbelow. When an electric current is charged to the device, the electricenergy is converted to a light energy thereby causing luminescence to beemitted in the form of a plane. Thus, the device has an ideal featurefor use as a display device of the spontaneous emission type.

FIG. 7 shows an example of a known organic EL device. An organic ELdevice 10 includes, on a transparent substrate 6 (e.g. a glasssubstrate), an ITO (indium tin oxide) transparent electrode 5, a holetransport layer 4, an emission layer 3, an electron transport layer 2,and a cathode 1 (e.g. an aluminium electrode) formed in this order, forexample, by a vacuum deposition method.

A DC voltage 7 is selectively applied between the transparent electrode5 serving as an anode and the cathode 1, so that holes serving ascarriers charged from the transparent electrode 5 are moved via the holetransport layer 4, and electrons charged from the cathode 1 are movedvia the electron transport layer 2, thereby causing the re-combinationof the electrons-holes. From the site of the re-combination, light 8with a given wavelength is emitted and can be observed from the side ofthe transparent substrate 6.

The emission layer 3 may be made of a light-emitting substance such as,for example, anthracene, naphthalene, phenanthrene, pyrene, chrysene,perylene, butadiene, coumarin, acridine, stilbene and the like. This maybe contained in the electron transport layer 2.

FIG. 8 shows another example of an organic EL device. In an organic ELdevice 20, the emission layer 3 as in FIG. 7 is omitted and, instead,such a light-emitting substance as mentioned above is contained in theelectron transport layer 2, and thus, the organic EL device 20 is soarranged as to emit light 18 having a given wavelength from an interfacebetween the electron transport layer 2 and the hole transport layer 4.

FIG. 9 shows an application of the organic EL device. More particularly,a built-up body of the respective organic layers (including the holetransport layer 4, and the emission layer 3 or the electron transportlayer 2) is interposed between the cathode 1 and the anode 5. Theseelectrodes are, respectively, provided in the form of stripes that areintersected in the form of a matrix. In this state, a signal voltage isapplied to in time series by means of a luminance signal circuit 34 anda shift register-built in control circuit 35 so that light is emitted ata number of intersected points (pixels), respectively.

Such an arrangement as set out above is usable not only as a display,but also as an image reproducing apparatus. It will be noted that if thestriped pattern is provided for the respective colors of R, G and B,there can be obtained a full color or a multi-color arrangement.

In a display device made of a plurality of pixels using the organic ELdevice, emitting organic thin film layers 2, 3 and 4 are usuallysandwiched between the transparent electrode 5 and the metal electrode1, and emission occurs at the side of the transparent electrode 5.

For use as constituting materials of the organic EL device, attentionhas now been drawn to organic luminescent materials and carriertransport materials suitable for use in combination with the organicluminescent materials. The advantages of these organic materials residein that their optical and electrical properties can be controlled tosome extent through the molecular design thereof. When an organicluminescent material having a given light emission and a carriertransport material suited therewith are used in combination, efficientlight emission is ensured. Accordingly, there can be realized a fullcolor organic EL device wherein primaries of R, G and B are emittedusing the respective luminescent materials.

In some case, such an organic EL device as set out above may have such astructure that a hole transport layer serves also as a luminescentelement. In this device structure, it is essential to provide a carriertransport layer that is able to efficiently transport electrons andblock holes. However, organic materials that satisfy the aboverequirement and the efficient manufacture of these materials have neverbeen found yet.

SUMMARY OF THE INVENTION

An object of the invention is to provide a novel organic material, whichis suitable for use as a carrier transport material capable ofefficiently transporting electrons and blocking holes.

Another object of the invention is to provide a process for preparingsuch an organic compound as mentioned above in an efficient manner.

According to an aspect of the invention, there is provided abathophenanthroline compound of the following general formula [I] or[II]

wherein R¹ and R² may be the same or different and independentlyrepresent a linear, branched or cyclic, saturated or unsaturatedhydrocarbon group, or a substituted or unsubstituted, saturated orunsaturated hydrocarbon group provided that at least one of R¹ and R²has at least two carbon atoms, or

wherein Ar¹ and Ar² may be the same or different and independentlyrepresent a substituted or unsubstituted aryl group.

The bathophenanthroline compound of the invention can control carriertransportability depending on the type of substituent introduced intothe molecule, and can thus be utilizable as a carrier transport materialof various types of organic EL devices. The compounds have high glasstransition point and high melting point and are stable electrically,thermally and/or chemically. In addition, the compounds are sublimablein nature, which is advantageous in that a uniform amorphous film can bereadily formed according to a vacuum deposition process.

In the bathophenanthroline compounds of the formulas [I] and [II], it ispreferred that R¹ and R², and Ar¹ and Ar² are, respectively, the same.It will be noted that the term “aryl group” used herein means acarbocyclic aromatic group such as, for example, a phenyl group, anaphthyl group, an anthryl group or the like, and a heterocyclicaromatic group such as, for example, a furyl group, a thienyl group, apyridyl group or the like.

According to another aspect of the invention, there is also provided aprocess for perparing a bathophenanthroline compound, which comprisingsubjecting a lithium compound of the following general formula [III] or[V]General Formula [III]:R³—Li or R⁴—Liwherein R³ and R⁴ may be the same or different and independentlyrepresent a linear, branched or cyclic, saturated or unsaturatedhydrocarbon group or a substituted or unsubstituted, saturated orunsaturated hydrocarbon group provided that at least one of R³ and R⁴has at least two carbon atoms, orGeneral Formula [V]:Ar³—Li or Ar⁴—Liwherein Ar³ and Ar⁴ may be the same or different and independentlyrepresent a substituted or unsubstituted aryl group, andbathophenanthroline of the following formula [IV]

to nucleophilic substitution reaction to obtain a bathophenanthrolinecompound of the afore-indicated formula [I] or [II].

According to the preparation process of the invention, thebathophenanthroline compound of the invention can be efficientlyprepared. It is preferred that in the course of the nucleophilicsubstitution reaction, carbanions are generated from the lithiumcompound and subsequently reacted with the bathophenanthroline.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic sectional view showing an essential part of anorganic EL device using a bathophenanthroline compound of the invention;

FIG. 2 is a schematic band model view showing a built-up structure ofthe organic EL device;

FIG. 3 is schematic sectional view showing a vacuum deposition apparatusused to make the organic EL device;

FIG. 4 is a plan view showing the organic EL device;

FIG. 5 is a schematic sectional view showing an essential part ofanother type of organic EL device using a bathophenanthroline compoundof the invention;

FIG. 6 is a schematic sectional view showing an essential part offurther another type of organic EL device using a bathophenanthrolinecompound of the invention;

FIG. 7 is a schematic sectional view showing an example of a prior-artorganic EL device;

FIG. 8 is a schematic sectional view showing an example of another typeof prior-art organic EL device; and

FIG. 9 is a schematic perspective view showing an example of furtheranother type of prior-art organic EL device.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The bathophenanthroline compound of the invention is described in moredetail. In the compound of the general formula [I] , R¹ and R²independently represent a linear, branched or cyclic, saturated orunsaturated hydrocarbon group. Specific examples include an ethyl group,a butyl group, an n-propyl group, an isopropyl group, an n-butyl group,a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentylgroup, a neopentyl group, a tert-pentyl group, a cyclopentyl group, ann-hexyl group, a 2-ethylbutyl group, a 3,3-dimethylbutyl group, acyclohexyl group, an n-heptyl group, a cyclohexylmethyl group, ann-octyl group, a tert-octyl group, a 2-ethylheyxl group, an n-nonylgroup, an n-decyl group, an n-dodecyl group, an n-tetradecyl group, ann-hexadecyl group and the like although not limited to thos mentionedabove.

Specific examples of the substituted or unsubstituted, saturated andunsaturated hydrocarbon group for R¹ and R² include a benzyl group, aphenethyl group, an α-methylbenzyl group, an α,α-dimethylbenzyl group, a1-naphthylmethyl group, a 2-naphthylmethyl group, a furfuryl group, a2-methylbenzyl group, a 3-methylbenzyl group, a 4-methylbenzyl group, a4-ethylbenzyl group, a 4-isopropylbnezyl group, a 4-tert-butylbenzylgroup, a 4-n-hexylbenzyl group, a 4-nonylbenzyl group, a3,4-dimethylbenzyl group, and the like saturated or unsaturatedhydrocarbon group although not limited to those mentioned above.

In the general formula [II], Ar¹ and Ar² independently represent asubstituted or unsubstituted aryl group. Specific examples include aphenyl group, a 1-naphthyl group, a 2-anthryl group, a 9-anthryl group,a 2-fluorenyl group, a 4-quinolyl group, a pyridyl group, a 3-pyridynylgroup, a 2-pyridynyl group, a 3-furyl group, a 2-furyl group, a3-thienyl group, a 2-oxazolyl group, a 2-thiazolyl group, a2-benzoxazoryl group, a 2-benzothiazoryl group, a 2-benzoimidazorylgroup, a 4-methylphenyl group, a 3-methylphenyl group, a 2-methylphenylgroup, a 2,3-dimethylphenyl group, a 2,4-dimethylphenyl group, a2,5-dimethylphenyl group, a 2,6-dimethylphenyl group, a3,4-dimethylphenyl group, a, 3,5-diemthylphenyl group, a2,3,4-trimethylphenyl group, a 2,3,5-trimethylphenyl group, a2,3,6-trimethylphenyl group, a 3,4,5-trimethylphenyl group, a4-ethylphenyl group, a 3-ethylphenyl group, a 2-ethylphenyl group, a2,3-diethylphenyl group, a 2,4-diethylphenyl group, a 2,5-diethylphenylgroup, a 2,6-diethylphenyl group, a 3,4-diethylphenyl group, a3,5-diethylphenyl group, a 2,3,4-triethylphenyl group, a2,3,5-triethylphenyl group, a 2,3,6-triethylphenyl group, a3,4,5-triethylphenyl group, a 4-n-propylphenyl group, a4-isopropylphenyl group, a 2-isopropylphenyl group, a 4-n-butylphenylgroup, a 4-isobutylphenyl group, a 4-sec-butylphenyl group, a4-tert-butylphenyl group, a 3-tert-butlphenyl group, a2-tert-butylphenyl group and the like although not limited to thosementioned above.

Specific examples of the bathophenanthroline compound of the inventionincludes those mentioned below as Compound Nos. 1 to 178, but thesecompounds should not be construed as limitation thereof. In the specificcompounds, Me represents a methyl group, Et represents an ethyl group,Pr represents a propyl group, and Bu represents a butyl group.

Preferred embodiments of the invention wherein bathophenanthrolinecompounds of the invention are, respectively, applied to an organic ELdevice are described.

FIRST EMBODIMENT

FIG. 1 is a schematic sectional view showing an essential part of anorganic EL device capable of emitting blue luminescence according to thefirst embodiment of the invention.

In this embodiment, a transparent electrode, made of ITO (indium tinoxide) or Zn-doped indium oxide, is formed on a glass substrate 6 bysputtering or vacuum deposition, followed by successively forming a holetransporting luminescent layer 4 a, a hole transporting luminescentlayer 4 b, a hole-blocking layer 33 containing a bathophenanthroline(derivative) compound of the afore-indicated general formula, anelectron transport layer 2, and a cathode electrode 1 in this orderaccording to a vacuum deposition technique to form an organic EL device(organic EL device) 21 made of the amorphous organic thin films.

This organic EL device 21 has such an arrangement that the holetransport layer 4 serves also as a luminescent layer, and thisfundamental structure is likewise employed in other embodimentsdescribed hereinafter.

The feature of the organic EL device 21 of this embodiment resides inthat the bathophenanthroline derivative-containing layer 33 isinterposed, as a hole-blocking layer, between the hole transport layer 4and the electron transport layer 2, so that the re-combination ofelectrons-holes is promoted in the hole transport layer 4, at whichluminescence is emitted, and/or luminescence is also emitted from thebathophenanthroline derivative-containing layer 33.

FIG. 2 schematically shows the built-up structure of the organic ELdevice of this embodiment in FIG. 1 as a band model.

In FIG. 2, the thick lines (L₁, L₂) indicated at the cathode 1 made ofAl and Al—Li (aluminium-lithium,) and the ITO transparent electrode 5layer, respectively, mean approximate work functions of the respectivemetals. In the respective layers between the electrodes, upper thicklines l₁, l₂, l₃ and l₄ and numerical values thereof indicate the lowestunoccupied molecular orbital (LUMO) levels, and lower thick lines l₅,l₆, l₇ and l₈ and numerical values thereof indicate the highest occupiedmolecular orbital (HOMO) levels, respectively. It is to be noted thatthe energy levels in FIG. 2 are shown only by way of example and maywidely vary depending on the types of materials.

In the organic EL device, as shown in FIG. 2, the holes h charged fromthe transparent electrode 5 serving as an anode are moved via the holetransport layer 4. On the other hand, electrons e charged from the metalelectrode 1 serving as a cathode are moved via the electron transportlayer 2. The electrons-holes are re-combined in the hole transportingluminescent layer, at which luminescence is emitted.

The electrons e charged from the metal electrode 1 serving as a cathodehas the tendency of moving toward a lower energy level, and can arriveat the hole transporting luminescent layers 4 b, 4 a via the lowestunoccupied molecular orbital (LUMO) levels l₁ to l₄ of the respectivelayers in the order of the metal electrode 1, electron transport layer2, hole-blocking layer 33, hole transporting luminescent layer 4 b andhole transporting luminescent layer 4 a.

On the other hand, the holes h charged from the ITO transparentelectrode 5 serving as an anode has the tendency of moving toward ahigher energy level, and can move to the electron transport layer 2 viathe highest occupied molecular orbital (HOMO) levels l₅ to l₇ of therespective layers in the order of the hole transporting luminescentlayer 4 a, hole transporting luminescent layer 4 b and hole-blockinglayer 33.

However, as shown in FIG. 2, the highest occupied molecular orbital(HOMO) level l₈ of the electron transport layer 2 is lower in energythan the highest occupied molecular orbital (HOMO) level 17 of thehole-blocking layer 33. This makes it difficult that the charged holes hmoves from the hole-blocking layer 33 toward the electron transportlayer 2, and thus, they are filled in the hole-blocking layer 33.

Eventually, the holes h filled in the hole-blocking layer 33 promote there-combination of electrons-holes at the hole transport layer 4, therebypermitting the luminescent materials of the hole transportingluminescent layers 4 a, 4 b or the hole transport layer 4 to emitluminescence or light.

In this way, the provision of the hole-blocking layer 33 effectivelycontrols the transport of the holes h in the hole-blocking layer 33 sothat the electron-hole re-combination in the hole transport layer 4 isefficiently caused. Thus, light with a specific wavelength (blue) isemitted in the form of light emission mainly from the hole transportingluminescent layer 4 b, adjoining to the hole-blocking layer 33, of thelight-emitting hole transporting luminescent layers 4 a, 4 b, to whichemission from the hole transporting luminescent layer 4 a is added.

Fundamentally, the electron-hole re-combination takes place in therespective layers including the electron transport layer 2 and the holetransport layer 4 as resulting from the charge of electrons from thecathode electrode 1 and the charge of holes from the anode electrode 5.Accordingly, in the absence of such a hole-blocking layer 33 as set outabove, the electron-hole re-combination occurs at the interface betweenthe electron transport layer 2 and the hole transport layer 4 so thatlight emission with a long wavelength alone is obtained. However, whenthe hole-blocking layer 33 as in this embodiment is provided, it isenabled to promote blue light emission while permitting the luminescentsubstance-containing hole transport layer 4 as an emission region.

As set out above, the hole-blocking layer 33 is provided to control thetransport of the holes h. To this end, it is sufficient that the highestoccupied molecular orbital (HOMO) level of the hole-blocking layer 33 isnot higher than the HOMO level that is lower in energy between the HOMOlevels of the hole transporting luminescent layer 4 b and the electrontransport layer 2, and that the lowest unoccupied molecular orbital(LUMO) level of the hole-blocking layer 33 is not lower than the LUMOlevel that is lower in energy and is not higher than the LUMO level thatis higher in energy, between the LUMO levels of the hole transportingluminescent layer 4 b and the electron transport layer 2. Thus, theinvention is not limited to such an arrangement as set out before.

In the practice of the invention, the energy levels may not always bewithin such ranges as defined before, and the bathophenanthrolinecompound-containing layer per se may emit light or luminescence. Inaddition, the hole-blocking layer may be made of a built-up structureincluding a plurality of layers.

The hole-blocking layer 33 may be formed of the bathophenanthrolinederivative and/or other material, and its thickness may be changedwithin a range permitting its function to be maintained. Moreparticularly, the thickness is preferably within a range of 1 Å to 1,000Å (0.1 nm to 100 nm). If the thickness is too small, the hole blockingability becomes incomplete, so that the re-combination region is liableto extend over the hole transport layer and the electron transportlayer. On the contrary, when the thickness is too large, light emissionmay not occur due to the increase in film resistance.

The organic EL device 21 is made by use of a vacuum deposition apparatus11 shown in FIG. 3. The apparatus 11 has therein a pair of support means13 fixed below an arm 12. A stage mechanism (not shown) is providedbetween the fixed support means 13 so that a transparent glass substrate6 can be turned down and a mask 22 can be set as shown. Below the glasssubstrate 6 and the mask 22, a shutter 14 supported with a shaft 14 a isprovided, below which a given number of deposition sources 28 arefurther provided. The deposition sources are heated by means of aresistance heating system using an electric power supply 29. For theheating, an EB (electron beam) heating system may also be used, ifnecessary.

In this apparatus, the mask 22 is for pixels, and the shutter 14 is fordeposition materials. The shutter 14 is able to rotate about the shaft14 a and has the function of intercepting a deposition stream of amaterial depending on the sublimation temperature of the depositionmaterial.

FIG. 4 is a plan view showing a specific example of the organic ELdevice fabricated by use of the vacuum deposition apparatus. Moreparticularly, ITO transparent electrodes 5 each with a size of 2 mm×2 mmare vacuum deposited on a glass substrate 6 with a size, L, of 30 mm×30mm by means of the vacuum deposition apparatus in a thickness of about100 nm, followed by vacuum deposition of SiO₂ 30 over the entire surfacethereof and etching in a given pixel pattern to form a multitude ofopenings 31. In this way, the transparent electrodes 5 are,respectively, exposed. Thereafter, the respective organic layers 4, 33,2 and a metal electrode 1 are successively formed through a depositionmask 22 of SiO₂ on each 2 mm×2 mm emission region (pixel) PX.

Using the vacuum deposition apparatus 11, a large-sized pixel may besingly formed, aside from the device having a multitude of pixels asshown in FIG. 4.

In this way, when the organic layer 33 is formed in order to improve theefficiency of the electron-hole re-combinations in the emission region,there can be obtained an organic EL device that is stable and high inbrightness, can be driven at a low voltage and has the hole transportingluminescent layer 4. As will be described in more detail, it is enabledto obtain a brightness of not smaller than 10,000 cd/m² by DC drive anda peak brightness, calculated as DC, of not smaller than 55,000 cd/m² bypulse drive at a duty ratio of 1/10 with respect to blue light emission.

The transparent electrode, organic hole transport layer, organichole-blocking layer, organic electron transport layer and metalelectrode of the electroluminescent device may, respectively, have abuilt-up structure made of a plurality of layers.

The respective organic layers of the electroluminescent device may beformed not only by vacuum deposition, but also other film-formingtechniques using sublimation or vaporization, or a technique of spincoating, casting or the like.

The hole transporting luminescent layer of the electroluminescent devicemay be formed by co-deposition of a small amount of molecules in orderto control emission spectra of the device, and may be, for example, anorganic thin film containing a small amount of an organic substance suchas a perylene derivative, a coumarin derivative or the like.

Usable hole transport materials include, aside from benzidine or itsderivatives, styrylamine or its derivatives and triphenylmethane or itsderivatives, porphyrin or its derivatives, triazole or its derivatives,imidazole or its derivatives, oxadiazole or its derivatives,polyarylalkanes or derivatives thereof, phenylenediamine or itsderivatives, arylamines or derivatives thereof, oxazole or itsderivatives, anthracene or its derivatives, fluorenone or itsderivatives, hydrazone or its derivatives, stilbene or its derivatives,or heterocyclic conjugated monomers, oligomers, polymers and the likesuch as polysilane compounds, vinylcarbazole compounds, thiophenecompounds, aniline compounds and the like.

More particularly, mention is made of α-naphthylphenyldiamine,porphyrin, metal tetraphenylporphyrins, metal naphthalocyanines,4,4′,4″-trimethyltriphenylamine,4,4′,4″-tris(3-methylphenylphenylamino)triphenylamine,N,N,N′,N′-tetrakis(p-tolyl)-p-phenylenediamine,N,N,N′,N′-tetraphenyl-4,4′-diaminobiphenyl, N-phenylcarbazole,4-di-p-tolylaminostilbene, poly(paraphenylenevinylene),poly(thiophenevinylene), poly(2,2′-thienylpyrrole) and the like,although not limited thereto.

Usable electron transport materials include quinoline or itsderivatives, perylene or its derivatives, bistylyl or its derivatives,pyrazine or its derivatives, and the like.

More specifically, mention is made, for example, of 8-hydroxyquinolinealuminium, anthracene, naphthalene, phenanthrene, pyrene, chrysene,perylene, butadiene, coumarin, acridine, stilbene, or derivativesthereof.

The materials used as the anode electrode or cathode electrode of theelectroluminescent device are not limitative in types.

The cathode electrode material should preferably be made of a metalwhose work function from a vacuum level of an electrode material issmall in order to efficiently charge electrons. There may be used, asidefrom an aluminium-lithium alloy, low work function metals such as, forexample, aluminium, indium, magnesium, silver, calcium, barium, lithiumand the like, singly or in the form of alloys with other metals forenhancing the stability thereof.

In order to take out organic electroluminescence from the side of theanode electrode, ITO is used as a transparent anode electrode inexamples appearing hereinafter. Nevertheless, there may be usedelectrode materials, which have a great work function from the vacuumlevel of an anode electrode material and include, for example, gold, astannic oxide-antimony mixture, a zinc oxide-aluminium mixture or thelike, so as to efficiently charge holes.

The substrate 2 may not be limited to a glass substrate, but may be madeof an opaque material. More particularly, there may be used, forexample, a silicon substrate, a Cr substrate, or a substrate made ofglass, on which a metal is formed by vacuum deposition. Where asubstrate made of an opaque material is used, it is preferred that theupper surface of an organic EL device (i.e. the side of the cathodeelectrode) is formed of a transparent or translucent material so thatelectroluminescence is picked out to outside. ITO may be used for thispurpose, for example.

There can be made an organic EL device for full color or multi-color,which is capable of emission of primaries of R, G and B, by properchoice of luminescent materials, not to mention an organic EL device formonochrome. Besides, the organic EL device of the invention is usablenot only for display, but also for light source along with itsapplication to other optical use.

It will be noted that the organic EL device may be sealed with germaniumoxide or the like so as to enhance the stability thereof by suppressingthe influence of oxygen or the like in air, or may be driven underconditions drawn to vacuum.

SECOND EMBODIMENT

FIG. 5 is a schematic sectional view showing an essential part of anorganic EL device according to a second embodiment of the invention. Anorganic EL device 22 of this embodiment differs from that of FIG. 1 inthat the hole transporting luminescent layer 4 b is formed on the ITOtransparent electrode 5 so that the hole transporting luminescent layeris formed as a single layer.

THIRD EMBODIMENT

FIG. 6 is a schematic sectional view showing an essential part of anorganic EL device according to a third embodiment of the invention.

An organic EL device 23 of this embodiment differs from that of FIG. 1in that a hole transport layer (serving also as a hole transportingluminescent layer) 4 a is formed on the ITO transparent electrode 5, andthus, the hole transporting luminescent layer is formed as a singlelayer, like the second embodiment.

The invention is more particularly described by way of examples.

EXAMPLE 1

<Preparation of 2,9-di(2-methylphenyl)bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 17.0 ml, 26.8 mmol) wasgradually dropped in an n-hexane solution (40 ml) of 2-iodotoluene (5.84g, 26.4 mmol) at room temperature. After completion of the dropping, thereaction solution was agitated at room temperature for 16 hours, and theresultant product was separated by filtration, followed by washing ofthe resulting white solid with n-hexane (40 ml×3 times) . A toluenesolution (50 ml) of bathophenanthroline (2.03 g, 6.11 mmol) wasgradually dropped, at room temperature, in an anhydrous diethylether/toluene (3:1) solution (20 ml) of the resulting white solid,followed by agitation at room temperature for 16 hours.

60 ml of iced water was added to the resultant reaction solution toseparate an organic layer therefrom. The aqueous layer was extractedthree times with chloroform, and the resultant organic layer was mixedwith the previously separated organic layer. 60 g of manganese dioxide(chemically treated product) was added to the thus mixed organic layerand agitated for 30 minutes, after which 100 g of sodium sulfate wasfurther added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=4:1→2:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (1.01 g, yield:49.5%) as light yellow crystals.

The product was identified through ¹H-NMR (solvent: chloroform) andFAB-MS measurements.

¹H-NMR: 2.70 (m, 6H, CH₃—Ar—), 7.25-7.75 (s, 18H, aromatic), 7.80 (s,2H, aromatic), 7.90 (s, 2H, aromatic)

MS: m/s (relative intensity) 512 (M⁺, 100)

The visible light absorption maximum wavelength of a tetrahydrofuran(THF) solution of the product was at 297 nm, with a fluorescentwavelength being at 390 nm.

EXAMPLE 2

<Preparation of 2,9-di(2,6-dimethylphenyl)-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 60.2 ml, 96.3 mmol) wasgradually dropped in an n-hexane/anhydrous diethyl ether (10:1) solution(110 ml) of 2-bromo-m-xylene (17.8 g, 96.3 mmol) at room temperature.After completion of the dropping, the reaction solution was heated underreflux for 2 hours and further agitated at room temperature for 16hours, and the resultant product was separated by filtration, followedby washing of the resulting white solids with n-hexane (50 ml×3 times).A toluene solution (80 ml) of bathophenanthroline (5.09 g, 15.3 mmol)was gradually dropped, at room temperature, in an anhydrous diethylether solution (40 ml) of the resulting white solids. After completionof the dropping, the solution was heated under reflux for 2 hours andagitated at room temperature for 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further add d, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (2.00 g, yield:39.4%) as light yellow crystals.

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 2.25 (m, 12H, CH₃—Ar—), 7.05 - 7.25 (s, 6H, aromatic), 7.35-7.70(s, 12H, aromatic), 7.95 (s, 2H, aromatic)

MS: m/s (relative intensity) 540 (M⁺, 100)

The visible light absorption maximum wavelength of a THF solution of theproduct was at 286 nm, with a fluorescent wavelength being at 380 nm.

EXAMPLE 3

<Preparation of 2,9-dinaphthyl-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 15.3 ml, 24.4 mmol) wasgradually dropped, at 0° C., in an n-hexane/anhydrous diethyl ether(1:1) solution (60 ml) of 1-bromonaphthalene (5.01 g, 24.4 mmol). Aftercompletion of the dropping, the reaction solution was agitated at roomtemperature for 16 hours, and the resultant product was subsequentlyseparated by filtration, and the residue was washed with n-hexane (40ml×3 times). A toluene solution (80 ml) of bathophenanthroline (2.03 g,6.11 mmol) was gradually dropped, at room temperature, in an anhydrousdiethyl ether solution (40 ml) of the resulting solids. After completionof the dropping, the reaction solution was agitated at room temperaturefor 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (1.38 g, yield:68.2%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 7.30-8.00 (s, 24H, aromatic), 8.32 (s, 2H, aromatic), 8.68 (s,2H, aromatic)

MS: m/s (relative intensity) 584 (M⁺, 100)

EXAMPLE 4

<Preparation of 2,9-difluorenyl-bathophenanthroline>

The reaction sequence is shown below

Lithium diisopropylamine (LDA)(1.89 g, 17.4 mmol) was added to a THFsolution (30 ml) of fluorene (4.16 g, 25.0 mmol) and agitated at roomtemperature for 16 hours. Thereafter, the THF and diisopropylamine wereremoved by distillation under reduced pressure. A toluene solution (60ml) of bathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped inan anhydrous diethyl ether solution (20 ml) of the resultant yellowsolids at room temperature. After the dropping, the reaction solutionwas heated under reflux for 2 hours and agitated at room temperature for16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (1.38 g, yield:68.2%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 4.51 (m, 2H, Ar—CH₂—Ar), 7.30-7.78 (s, 28H, aromatic), 7.81 (s,2H, aromatic)

MS: m/s (relative intensity) 660 (M⁺, 100)

EXAMPLE 5

<Preparation of 2,9-dibenzyl-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 4.45 ml, 7.13 mmol) wasgradually dropped in anhydrous toluene (2.24 g, 24.9 mmol) at roomtemperature. After completion of the dropping, Me-THF (0.627 g, 7.47mmol) was further added to the solution at −22° C. in 20 minutes.Thereafter, THF (1.06 g, 14.7 mmol) was added to in 30 minutes, followedby agitation at 6 to 10° C. for 16 hours. A toluene solution (40 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped, at roomtemperature, in the resultant reaction solution. After completion of thedropping, the reaction solution was agitated at room temperature for 16hours. 60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (0.88 g, yield:43.3%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 4.68 (m, 4H, —CH₂—Ar), 7.28-7.78 (s, 22H, aromatic), 7.81 (s,2H, aromatic)

MS: m/s (relative intensity) 512 (M⁺, 100)

EXAMPLE 6

<Preparation of 2,9-dicyclohexyl-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 36.3 ml, 58.0 mmol) wasgradually dropped, at room temperature, in an n-hexane/anhydrous diethylether (10:1) solution (50 ml) of chlorocyclohexane (3.00 g, 25.0 mmol).After completion of the dropping, the reaction solution was furtheragitated at room temperature for 16 hours, and the resultant product wassubsequently separated by filtration, and the resulting white solidswere washed with n-hexane (50 ml×3 times). A toluene solution (40 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped, at roomtemperature, in an anhydrous diethyl ether solution (10 ml) of theresulting white solids. After completion of the dropping, the reactionsolution was agitated at room temperature for 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (0.98 g, yield:48.3%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 0.80-2.45 (m, 20H, —CH₂—CH₂—CH₂—CH₂—CH₂—), 3.20 (m, 2H, —CH—Ar),7.25-7.75 (S, 12H, aromatic), 7.81 (s, 2H, aromatic)

MS: m/s (relative intensity) 496 (M⁺, 100)

EXAMPLE 7

<Preparation of 2,9-dibiphenyl-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 17.0 ml, 27.2 mmol) wasgradually dropped, at room temperature, in an n-hexane/anhydrous diethylether (10:1) solution (110 ml) of 4-boromobiphenyl (6.33 g, 27.2 mmol).After completion of the dropping, the reaction solution was agitated atroom temperature for 16 hours, and the resultant product wassubsequently separated by filtration, and the resulting white solidswere washed with n-hexane (50 ml×3 times) . A toluene solution (40 ml)of bathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped, atroom temperature, in an anhydrous diethyl ether solution (20 ml) of theresulting white solids. After completion of the dropping, the reactionsolution was agitated at room temperature for 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (0.76 g, yield:37.4%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 7.25-7.78 (s, 26H, aromatic), 7.81 (s, 2H, aromatic), 8.32 (s,4H, aromatic)

MS: m/s (relative intensity) 636 (M⁺, 100)

EXAMPLE 8

<Preparation of 2,9-di(2-methylbenzyl)-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 4.45 ml, 7.13 mmol) wasgradually dropped in α-bromo-o-xylene (4.91 g, 24.9 mmol) at roomtemperature. After completion of the dropping, Me-THF (0.627 g, 7.47mmol) was added in 20 minutes at −22° C., after which THF (1.06 g, 14.7mmol) was further added in 30 minutes, followed by further agitation at6 to 10° C. for 16 hours. A toluene solution (40 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped in theresultant reaction solution at room temperature. After completion of thedropping, the reaction solution was agitated at room temperature for 16hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (0.72 g, yield:35.4%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 2.35 (m, 6H, CH₃—Ar—), 4.65 (m, 4H, CH₂—Ar—) 7.25-7.78 (s, 20H,aromatic), 7.81 (s, 2H, aromatic) MS: m/s (relative intensity) 540 (M⁺,100)

EXAMPLE 9

<Preparation of 2,9-di(8-methylnaphthyl)-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 15.3 ml, 24.4 mmol) wasgradually dropped, at 0° C., in an n-hexane/anhydrous diethyl ether(1:1) solution (60 ml) of 1-bromo-8-methylnaphthalene (5.34 g, 24.4mmol). After completion of the dropping, the reaction solution wasagitated at room temperature for 16 hours, and the resultant product wassubsequently separated by filtration, and the residue was washed withn-hexane (40 ml×3 times). A toluene solution (80 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped, at roomtemperature, in an anhydrous diethyl ether solution (40 ml) of theresulting solids. After completion of the dropping, the reactionsolution was agitated at room temperature for 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (1.30 g, yield:64.0%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 2.60 (m, 6H, CH₃—Ar—), 7.30-7.81 (s, 22H, aromatic), 7.81 (s,2H, aromatic), 8.25 (s, 2H, aromatic)

MS: m/s (relative intensity) 612 (M⁺, 100)

EXAMPLE 10

<Preparation of 2,9-di(2-methylnaphthyl)-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 15.3 ml, 24.4.mmol) wasgradually dropped, at 0° C., in an n-hexane/anhydrous diethyl ether(1:1) solution (60 ml) of 1-boromo-2-methylnaphthalene (5.34 g, 24.4mmol). After completion of the dropping, the reaction solution wasagitated at room temperature for 16 hours, and the resultant product wassubsequently separated by filtration, and the residue was washed withn-hexane (40 ml×3 times). A toluene solution (80 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped, at roomtemperature, in an anhydrous diethyl ether solution (40 ml) of theresulting solids. After completion of the dropping, the reactionsolution was agitated at room temperature for 16 hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (1.20 g, yield:59.1%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 2.80 (m, 6H, CH₃—Ar—), 7.25-7.78 (s, 24H, aromatic), 7.81 (s,2H, aromatic)

MS: m/s (relative intensity) 612 (M⁺, 100)

EXAMPLE 11

<Preparation of 2,9-di(a-methylbenzyl)-bathophenanthroline>

The reaction sequence is shown below

n-Butyl lithium (1.6 M n-hexane solution, 4.45 ml, 7.13 mmol) wasgradually dropped in 1-bromo-1-phenylethane (4.91 g, 24.9 mmol) at roomtemperature. After completion of the dropping, Me-THF (0.627 g, 7.47mmol) was added in 20 minutes at −22° C., after which THF (1.06 g, 14.7mmol) was further added in 30 minutes, followed by further agitation at6 to 10° C. for 16 hours. A toluene solution (40 ml) ofbathophenanthroline (2.03 g, 6.11 mmol) was gradually dropped in theresultant reaction solution at room temperature. After completion of thedropping, the reaction solution was agitated at room temperature for 16hours.

60 ml of iced water was gradually added to the resultant reactionsolution to separate an organic layer therefrom. The aqueous layer wasextracted three times with chloroform, and the resultant organic layerwas mixed with the previously separated organic layer. 60 g of manganesedioxide (chemically treated product) was added to the thus mixed organiclayer and agitated for 30 minutes, after which 100 g of sodium sulfatewas further added, followed by agitation for 30 minutes.

The resulting mixed solution was filtered and concentrated, and theresidue was purified through column chromatography (silica gel,developing solvent: n-hexane/chloroform=8:1→4:1), followed byrecrystallization (solvent for recrystallization:chloroform/n-hexane=2:1) to obtain the intended compound (0.83 g, yield:40.9%).

The product was identified through ¹H-NMR and FAB-MS measurements.

¹H-NMR: 2.40 (m, 6H, CH₃—Ar—), 4.64 (m, 2H, —CH—Ar—), 7.25-7.78 (s, 22H,aromatic), 7.81 (s, 2H, aromatic)

MS: m/s (relative intensity) 540 (M⁺, 100)

As will be appreciated from the foregoing, the bathophenanthrolinecompounds of the invention can control, for example, carriertransportability depending on the type of substituent to be introducedinto the molecule, thus permitting one to utilize them as a carriertransport material of various types of organic EL devices. Moreover,these compounds have high glass transition point and melting point andare thus stable electrically, thermally and/or chemically. In addition,the compounds are sublimable in nature, thus leading to the advantagethat they are be readily formed as a uniform amorphous film according toa vacuum deposition process. The bathophenanthroline compound of theinvention can be efficiently prepared through nucleophilic substitutionreaction using an organolithium compound.

1-12. (canceled)
 13. An organic EL device comprising: an organic layerhaving a luminescent region provided between an anode and a cathode,wherein the organic layer comprises a bathophenanthroline compound offormula:

wherein Ar¹ and Ar² may be the same or different and independentlyrepresent an aryl group but do not form an interlocking macrocycliccompound.
 14. The bathophenanthroline compound according to claim 13wherein Ar¹ and Ar² are selected from the group consisting of a1-naphthyl group, a 2-anthryl group, a 9-anthryl group, a 2-fluorenylgroup, a 4-quinolyl group, a pyridyl group, a 3-pyridynyl group, a2-pyridynyl group, a 3-furyl group, a 2-furyl group, a 3-thienyl group,a 2-oxazolyl group, a 2-thiazolyl group, a 2-benzoxazoryl group, a2-benzothiazoryl group, a 2-benzoimidazoryl group, a 4-methylphenylgroup, a 3-methylphenyl group, a 2-methylphenyl group, an,n-dimethylphenyl group, a n,n,n-trimethylphenyl group, a n-ethylphenylgroup, a n,n-diethylphenyl group, a n,n,n-triethylphenyl group, a4-n-propylphenyl group, a n-isopropylphenyl group, a 4-n-butylphenylgroup, a 4-isobutylphenyl group, a 4-sec-butylphenyl group, an-tert-butylphenyl group.